01 1Central Glass Co., Ltd.
02 1Jiangsu Hengrui Pharmaceuticals Co. , Ltd.
01 1Sevoflurane
02 1Sevoflurane “Hengrui”
01 1China
02 1United Kingdom
Registration Number : 217MF10538
Registrant's Address : 5253 Okiube, Ube City, Yamaguchi Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2010-02-23
Registration Number : 231MF10009
Registrant's Address : No. 7, Kunlunshan Road, Economic and Technological Development Zone, Lianyungang, Jia...
Initial Date of Registration : 2019-01-10
Latest Date of Registration : 2019-01-10
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PharmaCompass offers a list of Sevoflurane API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sevoflurane manufacturer or Sevoflurane supplier for your needs.
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A fluoromethyl hexafluoroisopropyl ether manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of fluoromethyl hexafluoroisopropyl ether, including repackagers and relabelers. The FDA regulates fluoromethyl hexafluoroisopropyl ether manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. fluoromethyl hexafluoroisopropyl ether API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A fluoromethyl hexafluoroisopropyl ether supplier is an individual or a company that provides fluoromethyl hexafluoroisopropyl ether active pharmaceutical ingredient (API) or fluoromethyl hexafluoroisopropyl ether finished formulations upon request. The fluoromethyl hexafluoroisopropyl ether suppliers may include fluoromethyl hexafluoroisopropyl ether API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The fluoromethyl hexafluoroisopropyl ether Drug Master File in Japan (fluoromethyl hexafluoroisopropyl ether JDMF) empowers fluoromethyl hexafluoroisopropyl ether API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the fluoromethyl hexafluoroisopropyl ether JDMF during the approval evaluation for pharmaceutical products. At the time of fluoromethyl hexafluoroisopropyl ether JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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